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Merck

V900418

Sigma-Aldrich

Biotin

Vetec, reagent grade, ≥99%

Synonym(e):

D-Biotin, Bios II, Coenzym R, Vitamin B7, Vitamin H

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About This Item

Empirische Formel (Hill-System):
C10H16N2O3S
CAS-Nummer:
Molekulargewicht:
244.31
Beilstein:
86838
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352201
PubChem Substanz-ID:
Preise und Verfügbarkeit sind derzeit nicht verfügbar.

Qualität

reagent grade

Produktlinie

Vetec

Assay

≥99%

Form

powder

Farbe

white to off-white

mp (Schmelzpunkt)

231-233 °C (lit.)

Lagertemp.

2-8°C

SMILES String

[H][C@]12CS[C@@H](CCCCC(O)=O)[C@@]1([H])NC(=O)N2

InChI

1S/C10H16N2O3S/c13-8(14)4-2-1-3-7-9-6(5-16-7)11-10(15)12-9/h6-7,9H,1-5H2,(H,13,14)(H2,11,12,15)/t6-,7-,9-/m0/s1

InChIKey

YBJHBAHKTGYVGT-ZKWXMUAHSA-N

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Allgemeine Beschreibung

Biotin (vitamin B7 or vitamin H) is a water-soluble B complex vitamin, which consists of an uredo ring fused by a tetrahydrothiophene ring.[1] It is available in various foods, like whole grains, nuts, legumes, unpolished rice and egg yolk. Biotin is also produced by the normal gut flora.[2]

Biochem./physiol. Wirkung

Biotin is a vital cofactor for carboxylase enzymes in several metabolic pathways. It also functions as a coenzyme in the metabolism of fatty acids, isoleucine and valine. Biotin assists the transfer of carbon dioxide and also sustains a steady blood sugar level. Biotin is implicated in gluconeogenesis and citric acid cycle.[1] It is involved in keratin synthesis and hence is used as a supplement for skin, hair and nail growth.[2] Biotin is required for cell growth, production of fatty acids and the metabolism of fats and amino acids.[1]

Rechtliche Hinweise

Vetec is a trademark of Merck KGaA, Darmstadt, Germany

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 1

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


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Annals of Biological Research, 3(4), 1929-1933 (2012)
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Recently, we demonstrated that gap junction coupling in the population of superior coding ON-OFF directionally selective ganglion cells (DSGCs) genetically labeled in the Hb9::eGFP mouse retina allows the passage of lateral anticipatory signals that help track moving stimuli. Here, we
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Graphene related materials have been widely employed as highly efficient transducers for biorecognition. Here we show a conceptually new approach of using graphene oxide nanoplatelets (50 × 50 nm) as voltammetric inherently active labels for specific protein-target molecule recognition. This

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